216854-23-8 Usage
Description
(S)-3-N-Boc-aminopiperidine, also known as (S)-3-(tert-butoxycarbonyl)aminopiperidine, is a chiral organic compound that serves as a versatile intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is characterized by its white powder form and the presence of a Boc-protected amine group, which provides stability and reactivity in chemical reactions.
Uses
Used in Pharmaceutical Industry:
(S)-3-N-Boc-aminopiperidine is used as a key intermediate for the synthesis of chiral aminopiperidinyl quinolones, which are potent antibacterial agents effective against resistant pathogens. Its unique structure allows for the development of new drugs to combat antibiotic-resistant bacteria.
(S)-3-N-Boc-aminopiperidine is also used as an intermediate for the synthesis of alkynylpyrimidine amide derivatives, which are orally available inhibitors of Tie-2 kinase. These compounds have potential applications in the treatment of various diseases, including cancer and angiogenesis-related disorders.
Used in Agrochemical Industry:
(S)-3-N-Boc-aminopiperidine serves as an important raw material and intermediate in the synthesis of agrochemicals, contributing to the development of new pesticides and other agricultural products.
Used in Organic Synthesis:
(S)-3-N-Boc-aminopiperidine is a valuable intermediate in organic synthesis, enabling the creation of a wide range of chemical compounds with various applications.
Used in Pigment Industry:
(S)-3-N-Boc-aminopiperidine is used as an intermediate for pigments, playing a role in the development of new colorants for various industries, such as textiles, plastics, and paints.
Used in Dye Industry:
(S)-3-N-Boc-aminopiperidine contributes to the synthesis of dyes, expanding the range of color options and improving the properties of dyes used in different applications.
Check Digit Verification of cas no
The CAS Registry Mumber 216854-23-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,8,5 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 216854-23:
(8*2)+(7*1)+(6*6)+(5*8)+(4*5)+(3*4)+(2*2)+(1*3)=138
138 % 10 = 8
So 216854-23-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H20N2O2/c1-10(2,3)14-9(13)12-8-5-4-6-11-7-8/h8,11H,4-7H2,1-3H3,(H,12,13)/t8-/m0/s1
216854-23-8Relevant articles and documents
STEREOSELECTIVE SYNTHESIS OF PIPERIDINE DERIVATIVES
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Page/Page column 15, (2010/06/22)
This invention relates to dialdehyde or dinitrile compounds, which are useful for stereoselective synthesis of piperidine, pyrrolidine, and azepane derivatives.
An efficient conversion of chiral α-amino acids to enantiomerically pure 3-amino cyclic amines
Moon, Sung-Hwan,Lee, Sujin
, p. 3919 - 3926 (2007/10/03)
Enantiomerically pure 3-amino cyclic amines such as 3-amino pyrrolidine, 3-amino piperidine, and 2,3,4,5,6,7-hexahydro-1H-azepine have been synthesized in high yields from the optically active natural α-amino acids such as L-aspartic acid, L-glutamic acid, L-2-aminoadipic acid, and their enantiomers.